NDC 24385-804 Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
24385-804
Proprietary Name:
Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amerisourcebergen
Labeler Code:
24385
Start Marketing Date: [9]
05-24-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
ASPIRIN
Score:
1

Product Packages

NDC Code 24385-804-01

Package Description: 1 KIT in 1 KIT * .9 g in 1 PACKAGE (52124-0006-1) * .5 g in 1 TUBE (52124-0003-1) * 2 TABLET, CHEWABLE in 1 PACKAGE (52124-0012-1) * .5 mL in 1 PACKAGE (52124-0008-1) * .5 mL in 1 PACKAGE (52124-0002-1) * 10 mL in 1 BOTTLE (52124-0005-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .9 g in 1 PACKAGE (52124-0004-1)

Product Details

What is NDC 24385-804?

The NDC code 24385-804 is assigned by the FDA to the product Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces which is product labeled by Amerisourcebergen. The product's dosage form is . The product is distributed in a single package with assigned NDC code 24385-804-01 1 kit in 1 kit * .9 g in 1 package (52124-0006-1) * .5 g in 1 tube (52124-0003-1) * 2 tablet, chewable in 1 package (52124-0012-1) * .5 ml in 1 package (52124-0008-1) * .5 ml in 1 package (52124-0002-1) * 10 ml in 1 bottle (52124-0005-1) * .8 ml in 1 package (52124-0001-1) * .9 g in 1 package (52124-0004-1). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces?

This product is used as Purpose: First aid antiseptic, external analgesicUses: First aid to help prevent infection and for the temporary relief of pain and itching associated with: Minor CutsScrapesBurns Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water. Uses:  To help prevent infection in: minor cuts;  scrapes;  burns Uses:For flushing or irrigating the eyes toremove loose foreign material, air pollutants, or chlorinated water. Use:    For preparation of skin before injection. Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites. Usestemporary relief of minor aches, pains and headachesto reduce fever associated with colds, sore throats, teething Uses: For hand washing to decrease bacteria on the skin

Which are Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Good Neighbor Pharmacy Emergency Preparedness And First Aid Contains 167 Pieces?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
  • RxCUI: 1038561 - benzalkonium Cl 0.4 % Medicated Pad
  • RxCUI: 1038561 - benzalkonium chloride 4 MG/ML Medicated Pad

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".